Variant #0000609763 (NC_000005.9:g.64097126T>C, NC_000005.9(NM_005869.2):c.750-3T>C (CWC27))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.64097126T>C
DNA change (hg38) g.64801299T>C
Published as CWC27(NM_001297645.2):c.750-3T>C, CWC27(NM_005869.2):c.750-3T>C (p.?)
ISCN -
DB-ID CWC27_000015 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00116 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CWC27 NM_005869.2 -/. - c.750-3T>C r.spl? p.?


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